OBO ID: DOID:0050975
Term Name: spinocerebellar ataxia type 26 Search Ontology:
Synonyms:
Definition: An autosomal dominant cerebellar ataxia that is characterized by slowly progressive ataxia and oculomotor abnormalities, has_material_basis_in mutation in the EEF2 gene. https://rarediseases.info.nih.gov/diseases/9995/spinocerebellar-ataxia-26
References:
Ontology: Human Disease   ( DOID:0050975 )
Relationships
is a type of:
OTHER spinocerebellar ataxia type 26 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
EEF2 ?Spinocerebellar ataxia 26 609306
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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